Linked Data
ClinVar Variation Id:
588017
dbSNP Id:
rs138843201
ExAC:
1:151378877 G / C
gnomAD v2:
1-151378877-G-C
gnomAD v3:
1-151406401-G-C
gnomAD v4:
1-151406401-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.151406401G>C , CM000663.2:g.151406401G>C | GRCh38 |
| NC_000001.10:g.151378877G>C , CM000663.1:g.151378877G>C | GRCh37 |
| NC_000001.9:g.149645501G>C | NCBI36 |
| NG_046601.1:g.58065C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710270.1:c.2682C>G | ENSP00000518163.1:p.Ser894= | |
| ENST00000392723.6:c.2475C>G | ENSP00000376484.1:p.Ser825= | |
| ENST00000439756.2:c.2634C>G | ENSP00000390156.2:p.Ser878= | |
| ENST00000703168.1:c.2655C>G | ENSP00000515214.1:p.Ser885= | |
| ENST00000271715.7:c.2634C>G MANE Select | ENSP00000271715.2:p.Ser878= | |
| ENST00000271715.6:c.2634C>G | ENSP00000271715.2:p.Ser878= | |
| ENST00000358476.7:n.2782C>G | ||
| ENST00000368863.6:c.2349C>G | ENSP00000357856.2:p.Ser783= | |
| ENST00000392723.5:c.2475C>G | ENSP00000376484.1:p.Ser825= | |
| ENST00000409503.5:c.2607C>G | ENSP00000386836.1:p.Ser869= | |
| ENST00000491586.5:c.2502C>G | ENSP00000418408.1:p.Ser834= | |
| ENST00000529669.1:c.834C>G | ENSP00000432295.1:p.Ser278= | |
| ENST00000531094.5:c.2448C>G | ENSP00000431259.1:p.Ser816= | |
| NM_001194937.1:c.2607C>G | NP_001181866.1:p.Ser869= | |
| NM_001194938.1:c.2448C>G | NP_001181867.1:p.Ser816= | |
| NM_015100.3:c.2634C>G | NP_055915.2:p.Ser878= | |
| NM_145796.3:c.2349C>G | NP_665739.3:p.Ser783= | |
| NM_207171.2:c.2475C>G | NP_997054.1:p.Ser825= | |
| XM_005244999.1:c.2634C>G | XP_005245056.1:p.Ser878= | |
| XM_005245000.3:c.2634C>G | XP_005245057.1:p.Ser878= | |
| XM_005245001.1:c.2634C>G | XP_005245058.1:p.Ser878= | |
| XM_005245005.1:c.2475C>G | XP_005245062.1:p.Ser825= | |
| XM_005245006.3:c.2475C>G | XP_005245063.1:p.Ser825= | |
| XM_011509330.1:c.2526C>G | XP_011507632.1:p.Ser842= | |
| XM_011509331.1:c.2277C>G | XP_011507633.1:p.Ser759= | |
| XR_921760.1:n.2462C>G | ||
| XM_005244999.3:c.2634C>G | XP_005245056.1:p.Ser878= | |
| XM_005245000.4:c.2634C>G | XP_005245057.1:p.Ser878= | |
| XM_005245001.2:c.2634C>G | XP_005245058.1:p.Ser878= | |
| XM_005245005.2:c.2475C>G | XP_005245062.1:p.Ser825= | |
| XM_005245006.5:c.2475C>G | XP_005245063.1:p.Ser825= | |
| XM_017000744.1:c.2655C>G | XP_016856233.1:p.Ser885= | |
| XM_017000745.2:c.2607C>G | XP_016856234.1:p.Ser869= | |
| XM_017000746.1:c.2607C>G | XP_016856235.1:p.Ser869= | |
| XM_017000748.1:c.2475C>G | XP_016856237.1:p.Ser825= | |
| XM_017000749.1:c.2475C>G | XP_016856238.1:p.Ser825= | |
| XM_024454305.1:c.2508C>G | XP_024310073.1:p.Ser836= | |
| XM_024454306.1:c.1434C>G | XP_024310074.1:p.Ser478= | |
| XR_002959801.1:n.2489C>G | ||
| NM_015100.4:c.2634C>G MANE Select | NP_055915.2:p.Ser878= | |
| NM_001194937.2:c.2607C>G | NP_001181866.1:p.Ser869= | |
| NM_001194938.2:c.2448C>G | NP_001181867.1:p.Ser816= | |
| NM_145796.4:c.2349C>G | NP_665739.3:p.Ser783= |